Gene-specific Copy Number Variation Probe-MAGEL2
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| Catalog: |
CNVFP-MAGEL2-10910 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MAGEL2). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
MAGEL2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MAGEL2 genes. This product achieves the purpose of detection by hybridizing with the MAGEL2 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
MAGE Family Member L2 |
| Gene Summary [Provided by RefSeq] |
Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS. [provided by RefSeq, Oct 2010] |
| Gene Symbol |
MAGEL2 |
| Location |
15q11.2 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 23888695-23892993 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-MAGEL2-10910-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MAGEL2-10910-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MAGEL2-10910-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MAGEL2-10910-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MAGEL2-10910-AQ |
467nm |
418nm |
|
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